Sophia Millington‐Ward

RNA Interference–Mediated Suppression and Replacement of Human Rhodopsin In Vivo

Mary O’Reilly, Arpad Palfi, Naomi Chadderton et al. · The American Journal of Human Genetics · 2007 · 171 citations · Full text

Systems Biology, Molecular Physiology, Engineering +7

A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement

Sara J. Bowne, Marian M. Humphries, Lori S. Sullivan et al. · European Journal of Human Genetics · 2011 · 152 citations · Full text

Genome Instability, Mendelian Disorder, Genetic Disorder +10

Suppression and Replacement Gene Therapy for Autosomal Dominant Disease in a Murine Model of Dominant Retinitis Pigmentosa

Sophia Millington‐Ward, Naomi Chadderton, Mary O’Reilly et al. · Molecular Therapy · 2011 · 139 citations · Full text

Improved Retinal Function in a Mouse Model of Dominant Retinitis Pigmentosa Following AAV-delivered Gene Therapy

Naomi Chadderton, Sophia Millington‐Ward, Arpad Palfi et al. · Molecular Therapy · 2009 · 122 citations · Full text

Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene

Fiona C. Mansergh, Sophia Millington‐Ward, Avril Kennan et al. · The American Journal of Human Genetics · 1999 · 102 citations · Full text

C12258a Mutation, Mendelian Disorder, Mitochondrial Function +11